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Inflammatory myofibroblastic bladder tumor with divergent behavior in a patient with spinal cord injury

INTRODUCTION: An inflammatory myofibroblastic tumor of the bladder is rare. Some urothelial carcinoma with sarcomatoid changes may mimic an inflammatory myofibroblastic tumor. CASE PRESENTATION: A 76‐year‐old man with indwelling urinary catheters because of a spinal cord injury presented with gross...

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Detalles Bibliográficos
Autores principales: Tsuboi, Ichiro, Maruyama, Yuki, Sadahira, Takuya, Wada, Koichiro, Ando, Nobuyoshi, Mitsui, Yosuke, Nishiyama, Yasuhiro, Arata, Ryoji, Araki, Motoo, Nasu, Yasutomo, Ono, Noriaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292174/
https://www.ncbi.nlm.nih.gov/pubmed/32743416
http://dx.doi.org/10.1002/iju5.12085
Descripción
Sumario:INTRODUCTION: An inflammatory myofibroblastic tumor of the bladder is rare. Some urothelial carcinoma with sarcomatoid changes may mimic an inflammatory myofibroblastic tumor. CASE PRESENTATION: A 76‐year‐old man with indwelling urinary catheters because of a spinal cord injury presented with gross hematuria. Transurethral electrocoagulation and a resection were performed. A T2‐weighted magnetic resonance imaging showed a tumor and hematoma in the bladder diverticulum that pathologically resembled an inflammatory myofibroblastic tumor. This lesion was then removed en bloc by partial cystectomy. Histology showed a squamous cell carcinoma with sarcomatoid changes. After 4 months, a computed tomography showed the lesion had expanded outside the skin adjacent to the bladder. CONCLUSION: Some cases of inflammatory myofibroblastic tumors have a malignant course. Urologists therefore need to be aware of the possibility of rare cases of malignant bladder myofibroblasts.